A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891883



Internal ID19186279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:88408432..88499680hg38UCSC Ensembl
Outerchr10:88408432..88499680hg38UCSC Ensembl
Innerchr10:90168189..90259437hg19UCSC Ensembl
Outerchr10:90168189..90259437hg19UCSC Ensembl
Innerchr10:90158169..90249417hg18UCSC Ensembl
Outerchr10:90158169..90249417hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3891249
hg1991249
hg1891249
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798410
Samples
Known GenesRNLS
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891883
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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